Data Foundry

Medical device recalls 2019

SOMATOM go — Class II medical device recall Z-1915-2019

Terminated recall by Siemens Medical Solutions USA, Inc, reported 2019-07-10, distributed nationwide. The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user

Recall numberZ-1915-2019
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmSiemens Medical Solutions USA, Inc, Malvern, PA, United States
Recall initiated2019-05-28
Classified2019-07-02
Reported by FDA2019-07-10
Terminated2023-03-31
DistributedNationwide (US)
Quantity9
Serial numbers112519, 112536, 112541, 112542, 112545, 112551, 112552, 112555, 112573
Model numbers11061610

Product

SOMATOM go.Up (Model #11061610) with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as an aid in diagnosis. The images delivered by the system can be used by trained staff as an aid in diagnosis, treatment preparation and radiation therapy planning. This CT system can be used for low dose lung cancer screening in high risk populations. High risk populations are as defined by professional medical societies.

Reason for recall

The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user notifications. This may cause a delay in diagnosis or patient scans.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1915-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.